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Sec 5.8 - 5.11 notes
Sec 5.8 - 5.11 notes

... 1) Electrochemical cells convert __________ energy into ___________ energy. 2) ___________ is the electrode where oxidation occurs. 3) Electrons are ________ at the anode. 4) _________ is the electrode where reduction occurs. 5) In the half-rx at the cathode, e-‘s are on the ______ side of the equat ...
Equilibrium
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... energies, electronegativity and melting points for the alkali metals (Li  Cs), halogens (F  I) and period 3 elements (Na  Ar). Cross reference with topics 2, 4 and 5. Data for all these properties are listed in the data booklet. Explanations for the first four trends should be given in terms of t ...
Chemistry Name Mr. Reger Review Guide – Ch. 9
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... how can this be accomplished if they are traveling in a truck through different weather conditions? Also, when you receive your perishable product, how can you be certain that it has not been exposed to unfavorable conditions? It’s simple. You can use equilibrium. In water solutions, the Co 2 ion i ...
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... of a reaction experimentally by calorimetry, and for violent reactions by applying Hess’s Law to a series of reactions carried out separately in a calorimeter. These methods have lead to extensive tables listing the enthalpies of vaporization (∆Hvap), enthalpies of fusion (∆Hfus), enthalpies of redu ...
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... equation; order of reaction; rate constant; half-life of a reaction; rate-determining step b) Explain qualitatively, in terms of collisions, the effect of concentration changes on the rate of a reaction c) Explain that, in the presence of a catalyst, a reaction has a different mechanism, i.e. one of ...
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Photoredox catalysis



Photoredox catalysis is a branch of catalysis that harnesses the energy of visible light to accelerate a chemical reaction via a single-electron transfer. This area is named as a combination of ""photo-"" referring to light and redox, a condensed expression for the chemical processes of reduction and oxidation. In particular, photoredox catalysis employs small quantities of a light-sensitive compound that, when excited by light, can mediate the transfer of electrons between chemical compounds that otherwise would not react. Photoredox catalysts are generally drawn from three classes of materials: transition-metal complexes, organic dyes and semiconductors. While each class of materials has advantages, soluble transition-metal complexes are used most often.Study of this branch of catalysis led to the development of new methods to accomplish known and new chemical transformations. One attraction to the area is that photoredox catalysts are often less toxic than other reagents often used to generate free radicals, such as organotin reagents. Furthermore, while photoredox catalysts generate potent redox agents while exposed to light, they are innocuous under ordinary conditions Thus transition-metal complex photoredox catalysts are in some ways more attractive than stoichiometric redox agents such as quinones. The properties of photoredox catalysts can be modified by changing ligands and the metal, reflecting the somewhat modular nature of the catalyst.While photoredox catalysis has most often been applied to generate known reactive intermediates in a novel way, the study of this mode of catalysis led to the discovery of new organic reactions, such as the first direct functionalization of the β-arylation of saturated aldehydes. Although the D3-symmetric transition-metal complexes used in many photoredox-catalyzed reactions are chiral, the use of enantioenriched photoredox catalysts led to low levels of enantioselectivity in a photoredox-catalyzed aryl-aryl coupling reaction, suggesting that the chiral nature of these catalysts is not yet a highly effective means of transmitting stereochemical information in photoredox reactions. However, while synthetically useful levels of enantioselectivity have not been achieved using chiral photoredox catalysts alone, optically-active products have been obtained through the synergistic combination of photoredox catalysis with chiral organocatalysts such as secondary amines and Brønsted acids.
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